| Primary information |
|---|
| Hemolytik ID | 1506 |
| PMID | 20449481 |
| YEAR | 2010 |
| SEQUENCE | VOLRfPVOLfP |
| LENGTH | 11 |
| NAME | 3HCl (5) |
| C-ter Modification | Free |
| N-ter Modification | Free |
| Linear/Cyclic | Cyclic |
| Stereochemistry | Mix (Contains both L and D amino acids) |
| Modified Residues | Ornithine |
| FUNCTION | Antimicrobial |
| ACTIVITY | 15% hemolysis at 100μM |
| RBCs SOURCE | Sheep |
| Secondary information |
|---|
| Properties | Physico-Chemical details |
| STRUCTURE | |
| DSSP states | NA |
| SMILES | NA |
| External Links |
|---|
| PDB exact | PDB partial | SP exact | SP partial | TrEMBL exact | TrEMBL partial | IEDB exact | IEDB partial |
| NA |
NA |
NA |
NA |
NA |
NA |
NA |
NA |
|
| Reference Informaiton |
|---|
| ARTICLE | Antimicrobially active cycloundecapeptides related to gramicidin S having a novel turn structure with cis D-Phe-Pro peptide bond. |
| AUTHORS | Tamaki M,Sasaki I,Kokuno M,Shindo M,Kimura M |
| JOURNAL | Org Biomol Chem. 2010 Apr 21;8(8):1791-7. doi: 10.1039/b922159j. |
